Small ring compounds XX cyclopropyl radicals
✍ Scribed by Tatsuya Shono; Mitsumasa Akashi; Ryohei Oda
- Book ID
- 108385227
- Publisher
- Elsevier Science
- Year
- 1968
- Tongue
- French
- Weight
- 231 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Several experimental techniques have evolved to differentiate between two possible mechanisms of the thermal decomposition of oeroxv esters. These two mechanisms, the concerted and the non-concerted (Scheme I), have been investi-1 aated bv studvinq activation parameters , the effect on rates of deco
## Abstract 1‐Hydroxy‐ and 1‐halocyclopropyl sulfides can be conveniently prepared starting from cyclopropanone. Cyclopropyl sulfides with halogen or a dimethylsulfonium group in the α‐position can be transformed into 1‐substituted cyclopropyl sulfides with a variety of nucleophiles. This means tha
## Abstract 1‐Chlorocyclopropyl methyl ether and the corresponding sulfide are methanolysed without any rupture of the three‐membered ring. The solvolysis of 1‐halocyclopropyl sulfides has been studied kinetically and takes place __via__ an __S__~N~1 mechanism. Methyl substituents in the cyclopropy